Device recall
Z-2248-2010: REF 8788, 8mm C-REAMER, CANNULATED, STERILE, Rx ONLY. CONMED LINVATEC, 11311…
FDA device recall · Class II · Linvatec Corp. dba ConMed Linvatec
Key facts
| Recall number (Z-number) | Z-2248-2010 |
|---|---|
| Recall event | 54701 |
| Product | REF 8788, 8mm C-REAMER, CANNULATED, STERILE, Rx ONLY. CONMED LINVATEC, 11311 CONCEPT BLVD, LARGO, FL 33773-4908 USA. Intended for use in Arthroscopic knee procedures. |
| Product code | LXH |
| Recalling firm | Linvatec Corp. dba ConMed Linvatec |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 15, 2010 |
| FEI number | 1017294 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database